SLCTR/2011/002招募中未知
Intra cervical Foley catheter versus oral misoprostol for pre induction cervical ripening of post dated pregnancies. A randomized controlled trial
niversity of Ruhuna0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Consecutive women with uncomplicated singleton pregnancies having a cephalic presentation at period of gestation of 40 weeks and 6 days
排除标准
- •Complicated pregnancies – both maternal or fetal complications. Pregnancies with uncertain dates not confirmed by early scan, even though clinically considered as 41 weeks. Multiple pregnancies. Pregnancies with contraindication for normal vaginal delivery. Pregnancies with previous caesarean section. Women who have had insertion of intra cervical Foley catheter or vaginal PGE2 before 40 + 6 days. Contraindication for the use of misoprostol.
研究者
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